95898-05-8

Upstream product

• 18039-26-4 2,3,4-tri-O-benzyl-D-xylopyranose 
• 521304-45-0 phenyl 2,3,4-tri-O-acetyl-1-thio-1-deoxy-D-xylopyranoside 
• 62446-93-9 1,2,3,4-tetra-O-acetyl-D-xylopyranose 
• 87-72-9 D-Xylose 
• 100-39-0 benzyl bromide 
• 95898-04-7 1-O-acetyl 2,3,4-tri-O-benzyl-α,β-D-xylopyranose 

Downstream Products

• 95898-07-0 3β-cholesteryl 2,3,4-tri-O-benzyl-β-D-xylopyranoside 
• 95898-07-0 3β-cholesteryl 2,3,4-tri-O-benzyl-α-D-xylopyranoside 
• 37152-49-1 cholesteryl 3,4,6-tri-O-acetyl-β-D-gluco-pyranoside 
• 141883-06-9 C₅₈H₇₂O₁₄ 
• 141883-06-9 C₅₈H₇₂O₁₄ 
• 141883-00-3 Acetic acid (2R,3R,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-6-[(2S,4aR,5S,8aR)-5-(2-furan-3-yl-ethyl)-1,1,4a,6-tetramethyl-1,2,3,4,4a,5,8,8a-octahydro-naphthalen-2-yloxy]-5-hydroxy-tetrahydro-pyran-4-yl ester 
• 115243-86-2 Acetic acid (2R,3R,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-6-[(2S,4aS,8aR)-5-(2-furan-3-yl-ethyl)-1,1,4a,6-tetramethyl-1,2,3,4,4a,7,8,8a-octahydro-naphthalen-2-yloxy]-5-hydroxy-tetrahydro-pyran-4-yl ester 
• 115243-91-9 C₅₈H₇₂O₁₄ 
• 115243-91-9 C₅₈H₇₂O₁₄ 
• 115243-86-2 Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-6-[(2S,4aS,8aR)-5-(2-furan-3-yl-ethyl)-1,1,4a,6-tetramethyl-1,2,3,4,4a,7,8,8a-octahydro-naphthalen-2-yloxy]-5-hydroxy-tetrahydro-pyran-4-yl ester 
• 115243-91-9 C₅₈H₇₂O₁₄ 
• 115243-91-9 C₅₈H₇₂O₁₄ 
• 115243-91-9 C₅₈H₇₂O₁₄ 
• 115243-86-2 Acetic acid (2R,3R,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-6-[(2R,4aR,8aS)-5-(2-furan-3-yl-ethyl)-1,1,4a,6-tetramethyl-1,2,3,4,4a,7,8,8a-octahydro-naphthalen-2-yloxy]-5-hydroxy-tetrahydro-pyran-4-yl ester 

Relevant academic research and scientific papers

Synthesis of Glycosyl Fluorides by Photochemical Fluorination with Sulfur(VI) Hexafluoride

This study describes a new convenient method for the photocatalytic generation of glycosyl fluorides using sulfur(VI) hexafluoride as an inexpensive and safe fluorinating agent and 4,4′-dimethoxybenzophenone as a readily available organic photocatalyst. This mild method was employed to generate 16 different glycosyl fluorides, including the substrates with acid and base labile functionalities, in yields of 43%-97%, and it was applied in continuous flow to accomplish fluorination on an 7.7 g scale and 93% yield.

Stereoselective Glycosylation of Alcohols and Silyl Ethers Using Glycosyl Fluorides and Boron Trifluoride Etherate

The stereoselective glycosylation of alcohols and their silyl ethers has been achieved using O-alkyl-, O-acyl-, and acetal-protected glycosyl fluorides of the pyranose and furanose series and boron trifluoride etherate in CH2Cl2.